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Differential
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acanthocytosis
advances in neurology
akathisia
alcohol
alcohol, neurologic complications with
algorithm
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
Alzheimer's disease
Alzheimer's disease, familial
aminoacidopathies
aminoacidurias
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
anemia
anemia, hemolytic
anxiety
aphonia
apraxia
apraxia of eye movements
areflexia
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
athetosis, causes of
ATP1A3 gene
autonomic dysfunction
Babinski sign
baclofen
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
bicaudate index
biotin
blindness
blood dyscrasias, neurologic findings with
brain atrophy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcification, intracranial
carbamazepine
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, lesion of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortical atrophy
cerebrovascular accident
ceruloplasmin, serum
chewing movements
children
chorea
chorea, causes of
chorea, familial
chorea, familial benign
chorea, senile
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 19
chromosome 2
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clonazepam
cognition
confabulation
consanguinity
contractures, joint
copper metabolism, abnormal
cortical blindness
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
distal muscle atrophy
DNA probes
drooling
dying
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, paroxysmal
dystonia, treatment of
dystonic reaction, acute
electroencephalogram, abnormalities of
electromyogram
electron microscopy
emotional lability
employment
encephalopathy
enzyme, defect
epileptic encephalopathy
episodic neurologic deficits
equinovarus
ethics in neurology
exercise intolerance
exome sequencing
eye movement, disorders of
failure to thrive
familial
fasciculation
fatal familial insomnia
fever
flunarizine
fragile-X syndrome
Friedreich's ataxia
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
gliosis
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutaric acidemia
glutaric aciduria
grimacing
growth retardation
Hallervorden Spatz disease
hammertoes
handwriting
health insurance
hearing loss
hemiplegia
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, late onset
Huntington's chorea, membrane abnormality
Huntington's chorea, misdiagnosis of
Huntington's chorea, presymptomatic detection of
Huntington's chorea, sporadic form
Huntington's disease, children
hyperekplexia
hyperreflexia
hypertonia
hyporeflexia
hypotonia
imbalance
immunodeficiency
immunosuppression
impulsivity
inattention
inborn errors of metabolism
infantile bilateral striatal necrosis
insight, loss
insomnia
intellectual deficit
intellectual deterioration
internet
iron, brain
Jakob-Creutzfeldt disease
jaundice
karyotyping
Kayser-Fleischer ring
lactic acidemia
lenticular nucleus, lesion of, bilateral
Lesch-Nyhan syndrome
leukemia
leukodystrophy
lip, biting
lipid storage disorder of CNS
liver disease
liver function enzymes
liver transplantation
lymphocyte capping, diminished
lymphoma
lysosomal storage disease
manic-depressive
McLeod syndrome
memory, defect of recent
memory, impairment of
meningitis, carcinomatous
mental retardation
mental status, abnormal
metabolic disorder, primary
microcephaly
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
Minamata disease
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, eye of tiger sign
MRI, FLAIR
MRI, gradient-echo
MRI, paramagnetic effect
MRI, susceptibility weighted
multiple system atrophy
muscle stiffness
muscle weakness
muscular dystrophy
muscular dystrophy, Duchenne
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurofibromatosis 1
neurofibromatosis 2
neurologic disease
neurologic disease, diagnoses of
neurologic history
neurologic testing
neuronal migration disorder
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, peripheral
neurotoxin
neurotransmitter
next-generation sequencing
Niemann-Pick disease
nystagmus
nystagmus, gaze-evoked
nystagmus, monocular
ocular motility, disorders of
old age, neurology of
opened mouth
ophthalmoplegia
optic atrophy
optokinetic nystagmus, abnormal
palilalia
pancytopenia
PANK2 mutation
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal hemiplegia
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
pathology
penicillamine
peroxisomal disease
personality change
photosensitivity, skin
poison, mercury
poison, neurologic problems with
POLG1 gene
polymerase chain reaction
pons, atrophy
pontocerebellar atrophy
precipitating factors
prevention of neurologic disorders
prion disease
progeria
prognosis
progressive neurologic disorder
progressive pallidum atrophy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
putamen, lesion of
pyramidal tract
pyramidal tract dysfunction
quadriplegia
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recombinant DNA
recurrent
retinitis pigmentosa
review article
RFLPs
rigidity
salivation, excessive
schizophrenia
screening
sea-blue histiocytes
seizure
seizure, stimulus sensitive
self-mutilation
sensorineural hearing loss
short stature
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spasticity
speech disorder
speech disorder, childhood
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar degeneration
splenomegaly
startle reaction
status epilepticus
stereotypy
striatum, lesion of
striatum, lesion of, bilateral
striopallidodentate calcifications, familial idiopathic
substantia nigra
suicide
tardive dyskinesia
Tay-Sachs disease
telangiectases
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
tic
tongue, biting
torticollis
toxins, nervous system
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, wing beating
trinucleotide repeats
urea-cycle enzymopathies
uric acid, low
visual evoked response
walking, difficulty with
weight loss
wheelchair
white matter disease
wide based gait
workup
writers cramp
xeroderma pigmentosa
X-linked bulbospinal neuronopathy
Showing articles 1200 to 1250 of 1991 << Previous Next >>

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Syphilitic Meningomyelitis
Neurol 41:325-326, Strom,T.&Schneck,S.A., 1991

Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
Neurol 41:150-151, Sauter,M.K.,et al, 1991

Essential Tremor:Clinical Correlates in 350 Patients
Neurol 41:234-238, Lou,J.&Jankovic,J., 1991

The Effect of Flunarizine on Essential Tremor
Neurol 41:311-312, Biary,N.,et al, 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Nystagmus of Pelizaeus-Merzbacher Disease
Arch Neurol 48:87-91, Trobe,J.D.,et al, 1991

Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
Neurol 41:429-433, Baloh,R.W.&Winder,A., 1991

Corticosteroid-Responsive Dominantly Inherited Neuropathy in Childhood
Neurol 41:437-439, Bird,S.J.&Sladky,J.T., 1991

Lisch Nodules in Neurofibromatosis Type I
NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991

Clinicopath Conf
Pheochromocytoma of Adrenal Gland, Von Hippel-Lindau Disease, Case 16-1991, NEJM 324:1119-112791., , 1991

VonHippel-Lindau Disease
Editorial, Lancet 337:10651991., , 1991

Homocystinuria Due to 5, 10-Methylenetetrahydrofolate Reductase Deficiency Revealed by Stroke in Adult Siblings
Neurol 41:1313-1315, Visy,J.M.,et al, 1991

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Preliminary Report:Activation of the Cerebellum in Essential Tremor
Lancet 336:1028-1030, Colebatch,J.G.,et al, 1990

Recurrent Meningitis in a Patient with Congenital Deficiency of the C9 Component of Complement
Arch Int Med 150:2395-2399, Zoppi,M.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990

Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
Ann Neurol 28:585-588, Tietjen,G.E.&Drury,I., 1990

Conjugal Temporal Arteritis
Neurol 40:1839-1842, Galetta,S.L.,et al, 1990

Epilepsy Octet, Epidemiology, Classification, Natural History, and Genetics of Epilepsy
Lancet 336:93-96, Shorvon,S.D., 1990

Risk Factors for Multiple Sclerosis:Race or Place? Editorial
JNNP 53:821-823, 903, 906990., Compston,A., 1990

Multiple Sclerosis Sibling Pairs:Clustered Onset and Familial Predisposition
Neurol 40:1546-1552, Doolittle,T.H.,et al, 1990

Excessive Muscular Fatigue in Patients with Spastic Paraparesis
Neurol 40:1271-1274, Miller,R.G.,et al, 1990

Combined Resting-Postural Tremor of Lower Limbs:Another Essential Trem, or Variant
Neurol 40:1006, Rapoport,A.,et al, 1990

Prion Dementia Without Characteristic Pathology
Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Neurologic Sequelae of Open-Heart Surgery in Children
Am J Dis Child 144:369-373, Ferry,P.C., 1990

Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews
NEJM 323:6-12, Triggs-Raine,B.L.,et al, 1990

Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
Stroke 21:626-632, Schievink,W.I.,et al, 1990

Transvrse Myelitis and Spastic Paraparesis in a Patient with HIV Infection
NEJM 322:1322, Dodson,D., 1990

Familial Spastic Paraparesis Syndrome Associated with HTLV-I Infection
NEJM 323:732-737, Salazar-Grueso,E.F.,et al, 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
JNNP 53:644-648, Boughey,A.M.,et al, 1990

Electroencephalography Laboratory Diagnosis of Prolonged QT Interval
Ann Neurol 28:387-390, Gospe,S.M.&Gabor,A.J., 1990

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Abnormalities of Striatal Projection Neurons and n-Methyl-d-Aspartate Receptors in Presymptomatic Huntington's Disease
NEJM 322:1293-1298, Albin,R.L.,et al, 1990

Basal Ganglia Injury Aftr Cardiopulmonary Arrest:Clinical and Magnetic Resonance Imaging Correlation
Am J Dis Child 144:937-938, Jacobs,M.B.,et al, 1990

MRI in Familial Multiple Sclerosis
Neurol 40:900-903, Lynch,S.G.,et al, 1990

A Comparison of Sporadic and Familial Multiple Sclerosis
Neurol 40:1354-1358, Weinshenker,B.G.,et al, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Familial Meningioma
Neurol 40:312-314, McDowell,J.R., 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

A Large Kindred with Autosomal Dominant Parkinson's Disease
Ann Neurol 27:276-282, Golbe,L.I.,et al, 1990

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
NEJM 322:28-32, 541990., Krivit,W.,et al, 1990



Showing articles 1200 to 1250 of 1991 << Previous Next >>